Canonical Allele Identifier: PA2827972757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 420793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg88Trp
CA032840
NM_001354899.2:c.262C>T